Evidence map›Paper›PMID 22245967›Full record

ArticleNature structural & molecular biology2012

The splicing factor SRSF1 regulates apoptosis and proliferation to promote mammary epithelial cell transformation.

Olga Anczuków, Avi Z Rosenberg, Martin Akerman, Shipra Das, Lixing Zhan, Rotem Karni, Senthil K Muthuswamy, Adrian R Krainer

Abstract read
In one paragraph

Article in Nature structural & molecular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 292 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
292citing papers in PubMed, 1 pooled it
13.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

292 citing papers in PubMed, 1 synthesis or guideline pooled it, 464 citations in OpenAlex.

  1. Alternative splicing and cancer: a systematic review.Signal transduction and targeted therapy · 2021
    Pooled it
  2. SRSF3 plays a key role in liver cancer sex disparity by facilitating hepatocyte expression of ERα and FOXA.Proceedings of the National Academy of Sciences of the United States of America · 2026
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232 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 3 countries.

Olga AnczukówCold Spring Harbor Laboratory, Cold Spring Harbor, New York, USA.
Avi Z Rosenberg
Martin Akerman
Shipra Das
Lixing Zhan
Rotem Karni
Senthil K Muthuswamy
Adrian R Krainer
Cold Spring Harbor Laboratory · USHebrew University of Jerusalem · IL

Funding

VIRAL TRANSACTIVATIONP01CA013106 · NCI · COLD SPRING HARBOR LABORATORY · PI William Richard McCombie · 1985 to 2026
$116.8M
Early events of carcinoma induced by ErbB receptorsR01CA098830 · NCI · COLD SPRING HARBOR LABORATORY · PI MUTHUSWAMY, SENTHIL K · 2003 to 2013
$3.4M
Mechanisms by which Polarity Proteins Regulate Initiation and Progression of BreaR56CA098830 · NCI · COLD SPRING HARBOR LABORATORY · PI MUTHUSWAMY, SENTHIL K · 2008 to 2008
$240k
NCI NIH HHS CA098830NCI NIH HHS CA13106NCI NIH HHS P01 CA013106NCI NIH HHS R01 CA098830NCI NIH HHS R56 CA098830
6 · The paper itself

Abstract

The splicing-factor oncoprotein SRSF1 (also known as SF2/ASF or ASF/SF2) is upregulated in breast cancers. We investigated the ability of SRSF1 to transform human and mouse mammary epithelial cells in vivo and in vitro. SRSF1-overexpressing COMMA-1D cells formed tumors, following orthotopic transplantation to reconstitute the mammary gland. In three-dimensional (3D) culture, SRSF1-overexpressing MCF-10A cells formed larger acini than control cells, reflecting increased proliferation and delayed apoptosis during acinar morphogenesis. These effects required the first RNA-recognition motif and nuclear functions of SRSF1. SRSF1 overexpression promoted alternative splicing of BIM (also known as BCL2L11) and BIN1 to produce isoforms that lack pro-apoptotic functions and contribute to the phenotype. Finally, SRSF1 cooperated specifically with MYC to transform mammary epithelial cells, in part by potentiating eIF4E activation, and these cooperating oncogenes are significantly coexpressed in human breast tumors. Thus, SRSF1 can promote breast cancer, and SRSF1 itself or its downstream effectors may be valuable targets for the development of therapeutics.

Indexed as

Cell ProliferationCell Transformation, NeoplasticAnimalsApoptosisCell LineEpithelial CellsHumansMiceModels, BiologicalNuclear ProteinsOrgan Culture TechniquesRNA-Binding ProteinsSerine-Arginine Splicing FactorsNuclear ProteinsRNA-Binding ProteinsSerine-Arginine Splicing Factors

Identifiers

PMID22245967
PMCPMC3272117
OpenAlexW2000567082

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.